| Tag | Content |
|---|
EnhancerAtlas ID | HS182-01231 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:110777370-110779160 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GATA2 | MA0036.3 | chr1:110779120-110779131 | ACAGATAAGAA | - | 6.14 | | Gata1 | MA0035.3 | chr1:110779120-110779131 | ACAGATAAGAA | - | 6.62 | | JUND(var.2) | MA0492.1 | chr1:110778708-110778723 | GATGACCTCACTTTT | - | 6.05 | | Sox3 | MA0514.1 | chr1:110778878-110778888 | CCTTTGTTTT | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65653 | chr1:110775910-110779459 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I110234 | chr1 | 110777486 | 110779509 |
|
Enhancer Sequence | GCACCAGGCT CTGGCGGGTC TGGTTGCCTG CTTGCCTCTC CTTATTCTTG TCTTACTCCT 60
CACTCTTACT CTGGGCATCT GTGTAGGACC ATAGGGGCCT CAATTCAAAG TCTTGCTTTG 120
CTGCTTGCTA GCTGGGTGAC TTGGGGGTGA CTCACCGAAA TGGTTTCCCT GTTTGTTAGG 180
GAATAATGAT GGCCCCTGTT TCAGAGACAG AGTGAAGAGC CTGGCCTGGT GTCATGTGTC 240
TACCTGTGAT ATGACATATA GTAGCGGCAC AGTGTCAGCT CCCTCCCTGC CCTGTTCCTG 300
TCACTCTCAG ACTTTTCTCC ACAGACTTCT GAGATCTCCG TGTCCAGCTG CACCAAGAAA 360
GGACAAGAAC ACACCCGGGA GCTGTCTTGG GCAGTGTAGA ACAGCAGGGT GAGGACGGAA 420
TGGCCGAGGA GAGGGAAGAA GCCAGGGGAA GCCTGTTCCT GAAGTGTAAG GAAAGATCGG 480
GCTTGGAGCC TGGGCCAGCC GAGGCAAGGG GGTGGCAGGC AGCCAGTGTC AATTAAAGAT 540
AAAATTTCTC CTCCGGTAGT GGAGGGCAAA CAGTGGCTGT GGCCCCCCTA GACAGGAGAA 600
AGCCATTTGC AGCCAGGCTG GCCTTGGAAA AGCTTGGCCA GGCGATAATG GGACGGGATG 660
CGCTGCTGAC TCCATAATGA TATTACGCAT CAGGGCCCAC GGCCAAAGTG GCTGTTTTTT 720
CTGTAGATCG ATGTGGAACC ATTTCATGGT CAGGGGCTGA GAACCCAGCC AGCAGCAGGG 780
GTACTAGATG CCAGAGTGGT CCTGAGGGGA CTGAAGGGGT GGCAACTGGG GTCCCCAGTG 840
ACCGTTTCAG GCTGCTGGAA GAGGAGGGGG CAGTGTGCAG GAGGGTGGAG GGGTGGACGA 900
GAGAAGCAGC AGACTGCCCC TCCTCCCCAC CTCACAGAAA CAGCAGGCCG TGCTGTCAAG 960
GAAGAAAGGG CTCTGGCTTC CTCCTGTTCC CCAAAGCTGG AGTCGAGCCC AAGGTAGGGA 1020
GCTGGTTAAA AGAACAGGAC ATTGTTTAAA AGAATAAGAC AGACTTTTGA AGTCAGGCAG 1080
ACTTGGGTTT GAGTCCTGAC TCCATCACTT CCTTGTTGTG TGACCCTGGG CAAGTTACTC 1140
AGCCTCTGTG AACGTCTATT TCCTCATCTT TTAAATGTAG TATCTGCCTG AGGCCGTGTC 1200
TCTCTCATTG AGCCATGAGG AGAAATGAGT CGGCGCCTGT AAAGCCTCGC GCACAGTGCC 1260
TAGCACATAA CCATTGCTAG AGGGAGAGGG GAGTATTTTG GGGCAACTCA CTCCAGTAAC 1320
AGATGACCAG TTTGGTTTGA TGACCTCACT TTTCAGTGAA TCAGCCTCAT TTCACTGAAG 1380
TCCTTAGTCC TTATCTCCTT GTGAAGGAAT AAGAGGGGAT GATTATACCT AACAGCGAAC 1440
ATTTATTGAG TGCTGGGCAG TACATTTCAT GCTTATAAAG ATGCATTCCA AGATTGATGT 1500
TATCCTTACC TTTGTTTTAC GAGGAGAAAA CCAACACAAC AATGTCAGGT CATTTCTCCA 1560
AAGTCACACA GCCATTAAGT AGCAAAGCTG GGATTCAAAC TCAGTCTGGC TCTGTGGGTC 1620
CAATGCTTAG CCACTCTCTG AACTGAGTGG GGCTTGTGAG TCATAACCTC CAGTGTAGGA 1680
GTTTGTGCTT TTAGTGTTAT TTCCTTAACT GCAATTGATT CTCATAGCAA AGGTATTGTT 1740
TTCCCCTTTT ACAGATAAGA AACCAAGGCT TGGAGAAGTG AATCATTAAA 1790
|
